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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626931Generated: October 27, 2026

Water → tert-butyl N-(4-fluoropyridin-2-yl)carbamate

https://huagongshe.com/reaction/626931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl carbamateHCID 77922—
Reactant2-Chloro-4-fluoropyridineHCID 2782792—
Catalystpalladium(II) acetateHCID 167845—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl N-(4-fluoropyridin-2-yl)carbamateHCID 51354888128.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Palladium (II) acetate (1.69 g, 7.53 mmol) and Xantphos (8.71 g, 15.05 mmol) were dissolved/suspended in degassed 1,4-dioxane (1200 mL) in a nitrogen atmosphere. 2-Chloro-4-fluoropyridine (99 g, 753 mmol) and tert-butyl carbamate (97 g, 828 mmol) in 1,4-dioxane (550 mL) were added, followed by sodium hydroxide (45.2 g, 1.12 mol) and water (20 mL). The resulting mixture was heated at 100° C. for 2 h. The mixture was cooled to ambient temperature and filtered over celite. The residue was washed with 1,4-dioxane and the filtrate was concentrated to afford a yellow solid (206 g). The crude material was recrystallized from 2-propanol (400 mL) and dried to afford the title compound (120.8 g) as a white solid. LCMS 213 [M+H], RT 1.96 minutes, purity 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309243B2
Source datasetuspto-grants-2016_04
ORD IDord-f1c130313d444180b5c320f703a122dd
Source noteuspto-grants-2016_04